510(k) K151572 ยท HCG Device, Neurovascular Embolization
Penumbra Smart Coil
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Jul 10, 2015 |
| Received | Jun 11, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151572
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.